TERBUTALINE DOES NOT IMPROVE LUNG-FUNCTION IN PRETERM RABBITS

被引:1
作者
FIASCONE, JM
LI, MH
VREELAND, PN
机构
[1] NEW ENGLAND MED CTR,FLOATING HOSP INFANTS & CHILDREN,BOSTON PERINATAL CTR,BOSTON,MA 02111
[2] DARTMOUTH COLL,HITCHCOCK MED CTR,DARTMOUTH MED SCH,HANOVER,NH 03756
关键词
LUNG FUNCTION; TERBUTALINE; PREMATURE RABBITS;
D O I
10.1016/S0002-9378(11)91600-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: We used the premature rabbit model of surfactant deficiency to test the hypothesis that perinatal administration of terbutaline would lead to increased secretion of surfactant into the alveolar space and increase lung compliance during mechanical ventilation. STUDY DESIGN: Fetuses underwent delivery at a gestational age of 28 days (term 31 days) followed by mechanical ventilation. Fetuses were subdivided into four treatment protocols: control, fetuses given terbutaline at birth, fetuses of mothers given terbutaline 1 hour before delivery, and fetuses of mothers given terbutaline intramuscularly 12 hours before delivery. Dynamic compliance was determined. After this, alveolar lavage fluid was obtained for phosphatidylcholine content determination. Some fetuses were killed at birth and their alveolar lavage phosphatidylcholine was determined. RESULTS: Among the fetuses undergoing mechanical ventilation, perinatal terbutaline exposure did not alter either dynamic compliance or alveolar lavage phosphatidylcholine. Mechanical ventilaton was associated with large increases in alveolar lavage phosphatidylcholine content. CONCLUSION: Perinatal beta-adrenergic agonist exposure does not alter in vivo lung function following preterm delivery.
引用
收藏
页码:847 / 853
页数:7
相关论文
共 30 条
[1]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[2]   TERBUTALINE AND PULMONARY SURFACTANT RELEASE IN THE RABBIT FETUS [J].
BERGMAN, B ;
HEDNER, T ;
SAMSIOE, G .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 1982, 13 (01) :44-54
[3]   PRESSURE-VOLUME RELATIONSHIP AND FLUID CONTENT IN FETAL RABBIT LUNG AFTER BETA-RECEPTOR-STIMULATING DRUGS [J].
BERGMAN, B ;
HEDNER, T ;
LUNDBORG, P .
PEDIATRIC RESEARCH, 1980, 14 (09) :1067-1070
[4]   BETA-MIMETIC DRUGS AND POSSIBLE PREVENTION OF RESPIRATORY-DISTRESS SYNDROME [J].
BOOG, G ;
BRAHIM, MB ;
GANDAR, R .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1975, 82 (04) :285-288
[5]  
BRODY JS, 1986, HDB PHYSL RESPIRATOR, P335
[6]  
BROWN LAS, 1981, J BIOL CHEM, V256, P66
[7]  
CORBET A, 1983, AM REV RESPIR DIS, V128, P695
[8]   PULMONARY ALVEOLAR TYPE-II CELLS ISOLATED FROM RATS - RELEASE OF PHOSPHATIDYLCHOLINE IN RESPONSE TO BETA-ADRENERGIC STIMULATION [J].
DOBBS, LG ;
MASON, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1979, 63 (03) :378-387
[9]   INFLUENCE OF LONG-TERM BETA-MIMETIC THERAPY ON THE LECITHIN CONTENT OF AMNIOTIC-FLUID [J].
DUDENHAUSEN, JW ;
KYNAST, G ;
LANGELINDBERG, AM ;
SALING, E .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 1978, 9 (04) :205-209
[10]   GLUCOCORTICOIDS AND BETA-ADRENERGIC-RECEPTOR AGONISTS - THEIR COMBINED EFFECT ON FETAL RABBIT LUNG SURFACTANT [J].
EKELUND, L ;
ENHORNING, G .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1985, 152 (08) :1063-1067